Informaţii despre

Nume Long Qt Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli cardiovasculare
Boli din aceeaşi familie Familial Long Qt Syndrome; Long Qt Syndrome 1; Long Qt Syndrome 10; Long Qt Syndrome 11; Long Qt Syndrome 12; Long Qt Syndrome 13; Long Qt Syndrome 14; Long Qt Syndrome 15; Long Qt Syndrome 2; Long Qt Syndrome 3; Long Qt Syndrome 5; Long Qt Syndrome 6; Long Qt Syndrome 9

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Boli A-Z Acth Deficiency, Isolated Acute Dacryocystitis Adenoma Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Andersen Cardiodysrhythmic Periodic Paralysis Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Aplastic Anemia Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Asthma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Fibrillation Atrioventricular Block Autoimmune Hypoparathyroidism Autosomal Genetic Disease Beckwith-Wiedemann Syndrome Benign Neonatal Seizures Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Brain Cancer Branchiootic Syndrome 1 Breath-Holding Spells Brugada Syndrome Brugada Syndrome 2 Brugada Syndrome 5 Candidiasis Cardiac Arrest Cardiac Arrhythmia Cardiac Arrhythmia, Ankyrin-B-Related Cardiac Conduction Defect Cardiac Conduction Disease with or Without Dilated Cardiomyopathy Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 1p Catecholaminergic Polymorphic Ventricular Tachycardia Conduct Disorder Congenital Generalized Lipodystrophy Crouzon Syndrome with Acanthosis Nigricans Deafness, Autosomal Dominant 2a Deafness, Autosomal Recessive 44 Diabetes Mellitus Dilated Cardiomyopathy Duodenitis Dystonia 24 Endocarditis Epilepsy Epilepsy, Nocturnal Frontal Lobe, 1 Epithelial Recurrent Erosion Dystrophy External Ear Disease Fainting Familial Atrial Fibrillation Familial Long Qt Syndrome Familial Progressive Cardiac Conduction Defect Familial Short Qt Syndrome Familial Sick Sinus Syndrome Gastric Cancer Generalized Epilepsy with Febrile Seizures Plus Gestational Choriocarcinoma Goiter Heart Conduction Disease Heart Disease Helix Syndrome Hepatic Adenomas, Familial Hyperkalemic Periodic Paralysis Hyperparathyroidism Hypertrophic Cardiomyopathy Hypoglycemia Hypokalemia Hypokalemic Periodic Paralysis, Type 1 Hypoparathyroidism Ichthyosis Prematurity Syndrome Incontinentia Pigmenti Infective Endocarditis Intrinsic Cardiomyopathy Isolated Optic Neuritis Jervell and Lange-Nielsen Syndrome 1 Kearns-Sayre Syndrome Kindler Syndrome Kniest Dysplasia Leber Congenital Amaurosis 2 Left Ventricular Noncompaction Left Ventricular Noncompaction 1 Leukemia Lipodystrophy Lipodystrophy, Congenital Generalized, Type 4 Long Qt Syndrome 1 Long Qt Syndrome 12 Long Qt Syndrome 13 Long Qt Syndrome 14 Long Qt Syndrome 15 Long Qt Syndrome 2 Long Qt Syndrome 3 Long Qt Syndrome 5 Long Qt Syndrome 6 Long Qt Syndrome 9 Lymphoblastic Leukemia Malignant Spiradenoma Marfan Syndrome Meckel Syndrome, Type 1 Mitochondrial Dna Depletion Syndrome 4a Mucolipidosis Ii Alpha/beta Muscular Dystrophy Myopathy Otitis Externa Otomycosis Pancreatitis Periodic Paralyses Peripartum Cardiomyopathy Pituitary Hormone Deficiency, Combined, 2 Polyneuropathy Primary Hyperparathyroidism Progressive Familial Heart Block Propionic Acidemia Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Ramer Ladda Syndrome Renal Glucosuria Renal Hypoplasia Richards-Rundle Syndrome Right Bundle Branch Block Robinow Syndrome, Autosomal Recessive Second-Degree Atrioventricular Block Seizure Disorder Seizures, Benign Familial Infantile, 3 Seizures, Benign Familial Neonatal, 2 Short Qt Syndrome Spondyloocular Syndrome Spontaneous Ocular Nystagmus Sporotrichosis Sudden Arrhythmia Death Syndrome Sudden Infant Death Syndrome Supravalvular Aortic Stenosis Sveinsson Chorioretinal Atrophy Syncope Tetralogy of Fallot Thalassemia Third-Degree Atrioventricular Block Timothy Syndrome Triosephosphate Isomerase Deficiency Vaginitis Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy